Group 5 Transition Metal-Dinitrogen Complexes
Author:
Affiliation:
1. University of Maryland; Department of Chemistry and Biochemistry; 0300 Chemistry Building, 4418 Stadium Drive College Park MD 20742-2115 USA
Publisher
Wiley-VCH Verlag GmbH & Co. KGaA
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/9783527344260.ch3/fullpdf
Reference84 articles.
1. Metal-mediated production of isocyanates R3EN=C=O from dinitrogen, carbon dioxide, and R3ECl;Keane;Angew. Chem.,2015
2. Closing the loop on transition-metal-mediated nitrogen fixation: chemoselective production of HN(SiMe3)2 from N2, Me3SiCl, and X-OH (X = R, R3Si, or silica gel);Duman;J. Am. Chem. Soc.,2017
3. Dinitrogen activation at ambient temperatures: new modes of H2 and PhSiH3 additions for an “end-on-bridged” [Ta(IV)]2(μ-η1:η1-N2) complex and for the bis(μ-nitrido) [Ta(V)(μ-N)]2 product derived from facile N≡N bond cleavage;Hirotsu;J. Am. Chem. Soc.,2007
4. Fine-tuning the energy barrier for metal-mediated dinitrogen N≡N bond cleavage;Keane;J. Am. Chem. Soc.,2014
5. Extreme N≡N bond elongation and facile N-atom functionalization reactions within two structurally versatile new families of group 4 bimetallic “side-on-bridged” dinitrogen complexes for zirconium and hafnium;Hirotsu;J. Am. Chem. Soc.,2007
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